Výsledky vyhledávání - "Sunkada P. Rao"

Molecular Structures of Methyl 5,6-Diaryl-1,2,4-trimethyl-7-oxobicyclo[2.2.1]hept-5-en-2-endo-carboxylates (aryl = phenyl oro-methoxyphenyl)

Autor: Bubbly K Joseph, Mohan M Bhadbhade, Natarajan S Balasubrahmanyam, C. Sudarsanakumar, Sunkada P Rao

Publikováno v: Bulletin of the Chemical Society of Japan. 73:941-949

Structural assignments based on a reconstruction from the $^1H$ NMR dynamic behavior of the three 5,6-bis(substituted aryl)-7-oxo-5-norbornene-2-carboxylic esters named in the title have received confirmation from X-ray crystallographic studies. The

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2ebfa5ae0991cb1e6c70fa9d67831f3d
https://doi.org/10.1246/bcsj.73.941

Zobrazit plný text záznamu

Synthesis of C-glycosylarenes by way of internal reactions of benzylated and benzoylated carbohydrate derivatives

Autor: Stefanie A. Kane, Sunkada P. Rao, Amos B. Cutler, Prashant P. Deshpande, Olivier R. Martin, Carmen A.V. Hendricks

Publikováno v: Carbohydrate research. 196

“Internal” C -glycosylarenes [ e.g. , (2 R ,3 S ,3a S ,9b R )-3,3a,5,9b-tetrahydro-3-methoxy- and -3,7-dimethoxy-2-methoxymethyl-2 H -furo[3,2- c ][2]benzopyran] were prepared by intramolecular reactions of 2- O -benzyl derivatives of methyl 3,5-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4cf1920908c975dee699590f20c778b
https://pubmed.ncbi.nlm.nih.gov/2346943

Zobrazit plný text záznamu

C-glycosylation of substituted heterocycles under Friedel-Crafts conditions (I): a two-step synthesis of the thieno[3,4-]pyrimidine c-nucleoside analog of inosine

Autor: Kambhampati V. B. Rao, Robert S. Klein, Sunkada P Rao, Brian A. Otter, Wu-Yun Ran

Publikováno v: Tetrahedron Letters. 29:3537-3540

Direct stannic chloride catalyzed C-glycosylation of N-formyl-4-amino-3-carboalkoxy thiophenes with 1- O -acetyl-tri- O -benzoyl-β- D -ribofuranose, followed by annelation of a fused pyrimidone ring upon treatment with ammonia, constitutes a short a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::472db2f241b6b35c2b7a9138e9dd2804
https://doi.org/10.1016/0040-4039(88)85286-9

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání